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General Description Pharmacopoeia

What is the Pharmacopoeia? it is a mandatory book, contains all instructions for the correct identification of the medical compounds, published by the medical government authority or a medical Pharmaceutical Society. The descriptions of the preparations are called Monographs. It is a reference work for specifications of drugs.


BP British Pharmacopeia: Updated annually, the BP is the official, authoritative collection of standards for UK medicinal substances for human and veterinary use.


The BP includes almost 3,500 monographs which are legally enforced by the Human Medicines Regulations 2012. Where a pharmacopoeia monograph exists, medicinal products sold or supplied in the UK must comply with the relevant monograph. All monographs and requirements of the European Pharmacopoeia are also reproduced in the BP.


United States Pharmacopeia–National Formulary (USP–NF): The USP–NF features more than 4,900 monographs for drug substances, dosage forms, excipients, biologics, dietary supplements, and other therapeutics, plus General Chapters and harmonized material. USP–NF standards are used worldwide and are FDA-enforceable for drugs marketed in or exported to the United States. The USP–NF serves as a clear, step-by-step guide for chemical, physical, biological, and microbiological tests, procedures, and acceptance criteria for manufacturing and quality control. Available in English (print, online, and USB flash drive) and Spanish (print).


Cymit Química SL sale the USP - United States Pharmacopoeia, BP - British Pharmacopoeia Pharmacopoeia, EP - European Pharmacopoeia, JP Japan Pharmacopoeia, and many others, all available in our catalog. 


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